Clinical Development 招聘 在 中国 - 739 Job Positions Available

Job TitleClinical Development Scientist,IGT Job Description Job Responsibilities: • Analyzes clinical trial protocols and studies, ensuring adherence to regulatory requirements and alignment with strategic objectives, providing recommendations for protocol optimization and enhancement. • Crafts comprehensive and compliant Clinical Evaluation

Minimum Qualifications & Experience: Required Bachelors degree or equivalent in medicine, pharmacy, biology, or another related life science discipline. Minimum 10 years of experience within clinical research, drug development, or CRO environments. Demonstrated understanding of Phase I and

Job TitleClinical Development Scientist CT Job Description Job title: In this role, you will leverage your clinical and technical expertise to drive the development and growth of Philips CT business strategies. You will play a key role in shaping

Job TitleIntern - Clinical Development Assistant Job Description Job Description Job Responsibilities: According to the project plan and time requirements, work in the office or remotely, mainly completing the following tasks: 1. Manage and maintain the teams clinical evidence

Shanghai, China | full time | Job ID: 9282 Your main responsibilities are: Participate in the design and execution of clinical trials of their assigned programs, helping to create the clinical development plan for new compounds, and pave a

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,

Clinical Research Associate II, China ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Purpose: The Associate Director, Scientific Development supports and leads assigned customer- and commercial-focused strategic development engagements that accelerate business growth, customer impact, and coordinated scientific solutioning. This role connects customer needs,

Job Overview: The Senior Clinical Research Associate monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Company and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development solution

Novotech is a global full-service clinical Contract Research Organization (CRO). At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of

Novotech is a global full-service clinical Contract Research Organization (CRO). At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of

Job TitleAdvisory MR Clinical Scientist Job Description Your role: Collaborate with radiologists to conduct clinical application research on MR / AI, participate in the design of scientific research projects, follow-up on progress, contribute to SCI paper writing and

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing

Responsibilities Performing site evaluation, initiation, monitoring and close-out visits, plus maintaining appropriate documentation according to a project-specific monitoring plan, ICH-GCP, and applicable regulations. Supporting the development of a subject recruitment plan. Establishing regular lines of communication plus

Responsibilities Performing site evaluation, initiation, monitoring and close-out visits, plus maintaining appropriate documentation according to a project-specific monitoring plan, ICH-GCP, and applicable regulations. Supporting the development of a subject recruitment plan. Establishing regular lines of communication plus

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development solution

Job Description Responsible for scheduling and conduct of pre-study visits, initiation visits, interim monitoring visits and close-out visits according to the Monitoring Plan. Ensures the HGRAC and IRB submission and approval. Ensures assigned sites are conducting

About Human Pharmaceutical Business With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs of